HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241636Generated: October 31, 2026
Hydrochloric Acid → tert-Butyl 3-sulfanylazetidine-1-carboxylate
https://huagongshe.com/reaction/241636
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tert-butyl 3-(acetylthio)azetidine-1-carboxylate | HCID 18363257 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | tert-Butyl 3-sulfanylazetidine-1-carboxylate | HCID 58513580 | 101.3% |
Reaction Steps
Mixture of tert-butyl 3-(acetylthio)azetidine-1-carboxylate (STEP C, 700 mg, 3.03 mmol), methanol (10 mL) and potassium carbonate (836 mg, 6.05 mol) was stirred at 50° C. for 2 h and cooled to room temperature. To the reaction mixture was added 2 mol/L hydrochloric acid for solution acidified (pH <4). The resulting solution was extracted with diethyl ether (30 mL×2). The organic layer was combined and washed with water (30 mL×2) and brine (30 mL). The extract was dried with magnesium sulfate and concentrated. Resulting crude product (581 mg) was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653063B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-1976d53515af40f5b89eae1279a0532d |
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| Source note | uspto-grants-2014_02 |
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